Product Name Or Brand
Start broad with the product name, manufacturer, retailer brand or model family. This is usually the fastest way to find a possible notice.
Start with the product name or brand. If the list is too broad, search the exact UPC, lot code, model number, date code, NHTSA campaign number or official recall number printed on the notice or label.
Results help you find a possible match quickly. Before you stop use, discard, return or repair anything, open the official notice and confirm every affected detail.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
Workbless Pressure Washers Recalled Due to Risk of Serious Injury or Death from Shock and Electrocution Hazards
This recall involves Workbless-branded pressure washers, models WB0301 and WB0302. Model WB0301 is green and black and measures about 27.24 inches high, 10.83 inches wide and 8.39 inches deep. "WORKBLESS"," WB0301" and "ELECTRIC PRESSURE WASHER" are printed on a label on the back of the pressure washer. Model WB0302 is also green and black and measures about 29.57 inches high, 14.69 inches wide and 10.94 inches deep. "WORKBLESS", "WB0302" and "HEAVY DUTY ELECTRIC PRESSURE WASHER" are printed on a label on the back of the pressure washer. Both models came with four quick connect nozzles and a foam cannon.
|
CPSC
10936
|
Consumer Product | High |
Aug 20, 2026
Recall: Aug 20, 2026
|
Details |
Modine Manufacturing Company Recalls Airedale Heating and Cooling Ventilation Fans Due to Fire Hazard
This recall involves ventilation fans in ClassMate cooling and air source heat pumps and SchoolMate water/ground source heat pumps that supply heating, cooling and high indoor air quality in classrooms and schools in the following models: Model Ventilation Configuration (Digit 9) CMD C, D, or E CMP C, D, or E SMG H, J, K, N, or P SMW H, J, K, N, or P CMS H, J, K, N, or P The brand name Airedale is located on a sticker on the front of the unit. The model name and serial number are found on the serial plate on the underside of the control unit.
|
CPSC
10932
|
Consumer Product | Unknown |
Aug 20, 2026
Recall: Aug 20, 2026
|
Details |
KTM North America Recalls Off-Road Motorcycles Due to Risk of Serious Injury or Death from Crash Hazard
This recall involves 2021, 2022, 2023 and 2024 off-road motorcycles. The GASGAS off-road motorcycles are red with the white GASGAS logo on both sides of the shrouds. The Husqvarna motorcycles are white, blue and yellow with the Husqvarna logo on both sides of the shrouds. The VIN and number are located on the right side of the steering head. Recalled 2021, 2022, 2023 and 2024 Off Road Motorcycles Model Year Husqvarna Models 2022 FE 350 2022 FE 501 2022 TE 150i 2022 TE 250i 2022 TE 300i 2023 TE 150 2023 TE 250 2023 TE 300 2023 TE 300 Heritage 2023 FX 350 Heritage 2023 FX 350 2023 FE 450 2023 FE 450 Heritage 2023 FX 450 2023 TX 300 2023 TX 300 Heritage 2024 TE 150 2024 TE 250 2024 TE 300 2024 FE 350w 2024 FE 450 2024 FE 501w Model Year GASGAS Model 2021 EC 300 2022 EC 250 2022 EC 300 2023 EC 250 2023 EC 300 2023 EX 250 2023 EX 250F 2023 EX 300 2023 EX 350F 2023 EX 450F 2023 MC 125 2023 MC 250 2023 MC 250F 2023 MC 350F 2023 MC 450F 2024 MC 125 2024 MC 250 2024 MC 250F 2024 MC 350F 2024 MC 450F 2024 EC 250 2024 EC 300 2024 EC 450F 2024 EX 250 2024 EX 250F 2024 EX 300 2024 EX 350F 2024 EX 450F 2024 EW 500F
|
CPSC
10931
|
Consumer Product | High |
Aug 20, 2026
Recall: Aug 20, 2026
|
Details |
Koorlian Mattresses Recalled Due to Risk of Serious Injury or Death from Fire Hazard; Violate Mandatory Standard for Mattress Flammability; Sold on Amazon by Dream Bedding Technology
This recall involves Koorlian branded mattresses. The mattresses are 10 inches thick and were sold in a Twin XL size. They have a white top and blue sides and were sold compressed in a box. "Dreams Bedding Technology PTE LTD" the manufacture date and prototype ID "KY15Q290" are printed on a sewn-in white label located on one side of the mattress.
|
CPSC
10935
|
Consumer Product | High |
Aug 20, 2026
Recall: Aug 20, 2026
|
Details |
JINHEZO Mini Waterproof LED Tea Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries; Imported by Mystic ZO
This recall involves JINHEZO Mini Waterproof LED Tea Lights. The circular tea lights are clear with a white base and are about 1" in diameter and 1.14" tall. They come in a pack of 24 lights with 48 coin-cell batteries (two per light).
|
CPSC
10934
|
Child/Baby | High |
Aug 20, 2026
Recall: Aug 20, 2026
|
Details |
Goal Zero Recalls YETI 3000X Power Stations Due to Serious Risk of Injury from Fire and Burn Hazards
This recall involves Goal Zero's YETI 3000X power stations. The silver and black portable power stations measure about 24.4 inches high, 18.5 inches wide and 22.3 inches deep, and weigh about 92 pounds. The power stations have yellow handles and a digital display at the front with electrical ports. They sit on a rolling cart with two built-in wheels and a telescoping handle. The Goal Zero logo is printed on the front bar of the cart and on a nameplate located on the underside of the station's lid along with "YETI 3000X".
|
CPSC
10933
|
Consumer Product | Medium |
Aug 20, 2026
Recall: Aug 20, 2026
|
Details |
CCM Hockey U.S. Recalls FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories Due to Risk of Injury from Laceration or Impact Hazards
This recall involves the CCM Hybrid Hockey Visors, style FMHVR and replacement visor accessories, style ACCHVR. The recalled FMHVR Hybrid Visors are marked "HVR" at the top of the metal plate (above "CCM" in red). Recalled FMHVR visors have serial numbers beginning with "M/L" or "S/M." The recalled ACCHVR Replacement Visor accessory has serial numbers beginning with "SR". The serial number is printed at the top corner on the right- hand-side metal plate where HVR - CCM are written, inside of the visors, engraved into the polycarbonate. The following visor and visor accessories are included in the recall. Recalled Visors and Visor Accessories: S/M FMHVR SR CCM CAG Visor Black Chrome S/M M/L FMHVR SR CCM CAG Visor Black Chrome M/L M/L ACCHVR CONTAINS REPLACEMENT VISOR(1) + SIDE CLIPS(2) + SPACERS(2) + SCRFEWS(2) S/M ACCHVR CONTAINS REPLACEMENT VISOR(1) + SIDE CLIPS(2) + SPACERS(2) + SCRFEWS(2)
|
CPSC
10937
|
Consumer Product | Medium |
Aug 20, 2026
Recall: Aug 20, 2026
|
Details |
|
ADS Software May Cause Unexpected Vehicle Movement
Avride Inc. (Avride) is recalling certain Automated Driving Systems (ADS) equipped with software versions prior to RC-01-05. The ADS software may direct the vehicle to change lanes, merge, or veer left or right without yielding or maintaining a safe distance from other vehicles. Unexpected vehicle movement may increase the risk of a crash.
|
NHTSA
26E059000
|
Vehicle | High |
Aug 19, 2026
Recall: Aug 19, 2026
|
Details |
|
Hydraulic Valve May Fail and Prevent Outrigger Operation
E-One Incorporated (E-One) is recalling certain 2026 Cyclone 2, 2025-2026 Cyclone, and Typhoon fire trucks. The hydraulic valve may become inoperative, preventing the outriggers from being extended or retracted. The inability to extend or retract the outriggers can delay emergency response, increasing the risk of injury.
|
NHTSA
26V537000
|
Vehicle | Medium |
Aug 19, 2026
Recall: Aug 19, 2026
|
Details |
|
FDA
H-1229-2026
|
Food | High |
Aug 19, 2026
Recall: Jul 22, 2026
|
Details | |
|
Vodka Tomato Sauce, NET WT. 24 oz / 680g, glass jar packed 12 jars in a carton.
Label declares cream and cheese, but Milk is not declared
|
FDA
H-1224-2026
|
Food | High |
Aug 19, 2026
Recall: Jul 23, 2026
|
Details |
|
FDA
H-1225-2026
|
Food | High |
Aug 19, 2026
Recall: Jul 28, 2026
|
Details | |
|
FDA
H-1228-2026
|
Food | High |
Aug 19, 2026
Recall: May 23, 2026
|
Details | |
|
FDA
H-1230-2026
|
Food | High |
Aug 19, 2026
Recall: Jul 22, 2026
|
Details | |
|
Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222,722223, 722224, 722225, 722226, 722227, 722228, 722280*, 722281*, and 722282* (*These models are distributed only in China), with Software Version Number R2.2.10 and R2.1.10* (*This software version is distributed only in China); Interventional Fluoroscopic X-Ray System
Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate treatment and 2) Potential loss of geometry movements that may lead to delay of therapy and procedural complications
|
FDA
Z-2931-2026
|
Medical Device | High |
Aug 19, 2026
Recall: Jul 16, 2026
|
Details |
|
BIOFIRE Respiratory Panel 2.1 (RP2.1) REF 423742 UDI code: 00815381020529 PCR-based multiplexed nucleic acid test, in vitro diagnostic
Due to increase in false negative results
|
FDA
Z-2936-2026
|
Medical Device | High |
Aug 19, 2026
Recall: Jun 24, 2026
|
Details |
|
OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1
There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions for both the patient and the healthcare provider.
|
FDA
Z-2933-2026
|
Medical Device | High |
Aug 19, 2026
Recall: Jul 13, 2026
|
Details |
|
Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31 DERMALON* 4-0 BLU 75CM C14 88861799-31
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if in ophthalmic utilization, or prolonged surgery.
|
FDA
Z-2920-2026
|
Medical Device | High |
Aug 19, 2026
Recall: Jun 24, 2026
|
Details |
|
Cardinal Health Presource Kits: 1) BASIC PACK , Catalog Number: SBA73BPGCA; 2) SPINE PACK , Catalog Number: SNE11SPHKC; 3) SPINE PACK , Catalog Number: SNE11SPHKD; 4) CRANIOTOMY PACK , Catalog Number: SNE12BS01B
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
|
FDA
Z-2949-2026
|
Medical Device | High |
Aug 19, 2026
Recall: Jul 14, 2026
|
Details |
|
Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if in ophthalmic utilization, or prolonged surgery.
|
FDA
Z-2921-2026
|
Medical Device | High |
Aug 19, 2026
Recall: Jun 24, 2026
|
Details |
|
ProNephro AKI (NGAL) Reagent Kit (100 tests). IVD Acute Kidney Injury Test System.
The use of a non-validated rework process for assay reagents which could lead to missed diagnosis of renal disease, inappropriate treatment decisions, or inappropriate monitoring of renal disease in intended users.
|
FDA
Z-2937-2026
|
Medical Device | High |
Aug 19, 2026
Recall: May 18, 2026
|
Details |
|
GM Helix Implant, Endosseous Dental Implant Article No. 109.984
There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the incorrect implant is installed, the issue could cause bone compression or difficulty during installation in situations where there is sufficient bone volume
|
FDA
Z-2929-2026
|
Medical Device | High |
Aug 19, 2026
Recall: Jul 13, 2026
|
Details |
|
Cardinal Health Presource Kits: 1) SEPTO RHINO PACK , Catalog Number: SEN73NSKCF; 2) PACK NEURO MINOR CRANIOTOMY , Catalog Number: SNE30CNOHE; 3) NEURO MAJOR 2 PACK , Catalog Number: SNE30CRJGY; 4) NEURO PACK , Catalog Number: SNE43NEE13; 5) LAMINECTOMY PACK , Catalog Number: SNE43NEE13; 7) LAMINECTOMY PACK , Catalog Number: SNE5CLPB13; 8) PEDI SPINE R , Catalog Number: SNE69PSKR4; 9) SHUNT PACK , Catalog Number: SNE7CSHY15; 10) SHUNT PACK , Catalog Number: SNE7CSHY16; 11) ENS ORTHO FUSION POSTERIEURE 3, Catalog Number: SOP30ODSCL
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
|
FDA
Z-2946-2026
|
Medical Device | High |
Aug 19, 2026
Recall: Jul 14, 2026
|
Details |
|
Endo-Model, Replacement Set, Tibial Plateau, right/left, L, UHMWPE, CoCrMo, Rotating Hinge Item Number 15-0027/16
The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau. The incorrect plateau could lead to a prolonged or modified surgery as the plateau cannot be inserted and an alternative product would be needed. If the incorrect plateau were to be implanted, this is associated with increased risk of wear, which could result in a reduced standing time of the implant.
|
FDA
Z-2934-2026
|
Medical Device | High |
Aug 19, 2026
Recall: Jul 6, 2026
|
Details |
|
60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site REF MPX5305-C UDI-DI code: 10885403274619 9 IN Extension Set w/Max Y REF MPX5300-C UDI-DI code: 10885403237218 Intravascular Administration Set and Extension Set used to administer fluids.
Products may not have received adequate sterilization processing.
|
FDA
Z-2941-2026
|
Medical Device | High |
Aug 19, 2026
Recall: Jun 16, 2026
|
Details |
Use brand, product name, UPC, lot code, best-by date, package size, allergen, contamination issue or distribution state.
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For appliances, electronics, toys, furniture and baby products, match the model number, serial range, date code, color, size and retailer listing.
This site can find vehicle recall campaigns. For your exact car, use the official NHTSA VIN lookup to confirm unrepaired recall status.
Consumer products, toys, furniture, appliances, electronics and baby products. CPSC remedy details can change after a notice is first posted.
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Meat, poultry and egg product recalls and public health alerts. Check establishment numbers, lot codes, labels and affected states.
Vehicle, tire, equipment and child-seat campaigns. VIN or license plate lookup is needed to know whether your specific vehicle still needs repair.
Use the brand, product name, manufacturer or retailer. If the result list is long, add a code from the label or package.
Read the product description, recall reason, hazard, affected dates, source agency and official recall number before taking action.
Compare the UPC, lot, best-by date, establishment number, model, serial range, color, size, state, retailer and product photo.
The notice may say stop using, do not eat, discard, return for refund, request a repair kit, replace a part or schedule dealer service.
Do not rely on brand alone. Match the package size, UPC, lot code, best-by date, use-by date, distribution states and any allergy or contamination warning.
Look for model number, date code, serial range, color, size, online listing, product photo and the exact hazard such as choking, suffocation, fire or fall risk.
Use campaign results to understand the issue, then verify your VIN, car seat model or tire information with NHTSA or the manufacturer.
Your item may not be part of that specific recall. Check spelling, older notices, retailer alerts and the official source before deciding it is safe.
A product recall is a safety or compliance notice saying a product may need to be corrected, removed, returned, repaired, replaced, refunded or discarded.
If all affected details match, follow the official instructions. Keep packaging, take photos, save receipts and contact the company or retailer when a refund or repair is offered.
A similar brand or product name is not enough. UPCs, lot codes, dates, model numbers, serial ranges and distribution areas determine whether your item is included.
Be careful with text messages, social posts or refund forms that ask for private information. Verify the notice through an official agency, retailer or manufacturer page.
Yes, when the official recall notice includes a UPC or product code. If no result appears, also search the brand, product name, package size, lot code and company name.
Yes. Lot codes are especially useful for food, drug, cosmetic and pet food recalls because only certain production batches may be affected.
No. This tool helps find vehicle recall campaigns and NHTSA numbers. Use the official NHTSA VIN or license plate lookup for vehicle-specific unrepaired recall status.
The database combines multiple official U.S. sources, but agencies and companies can publish or update notices at different times. Always check the linked official notice before taking final action.